Canonical Allele Identifier: CA421068354

Gene: LMNA

Linked Data

• MyVariant Identifiers: chr1:g.156100543T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156130752T>C , CM000663.2:g.156130752T>C	GRCh38
NC_000001.10:g.156100543T>C , CM000663.1:g.156100543T>C	GRCh37
NC_000001.9:g.154367167T>C	NCBI36
NG_008692.2:g.53180T>C , LRG_254:g.53180T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504687.7:c.-67T>C	ENSP00000426535.3:n.-67T>C
ENST00000682650.1:c.492T>C	ENSP00000506904.1:p.Asp164=
ENST00000683032.1:c.492T>C	ENSP00000506771.1:p.Asp164=
ENST00000684195.1:c.492T>C	ENSP00000508220.1:p.Asp164=
ENST00000361308.9:c.492T>C	ENSP00000355292.6:p.Asp164=
ENST00000368300.9:c.492T>C MANE Select	ENSP00000357283.4:p.Asp164=
ENST00000496738.6:n.867T>C
ENST00000504687.6:c.-173T>C	ENSP00000426535.2:n.-173T>C
ENST00000674518.1:c.492T>C	ENSP00000502261.1:p.Asp164=
ENST00000674600.1:c.*291T>C	ENSP00000501666.1:n.*291T>C
ENST00000674720.1:c.492T>C	ENSP00000502798.1:p.Asp164=
ENST00000675431.1:n.185T>C
ENST00000675455.1:c.*292T>C	ENSP00000501795.1:n.*292T>C
ENST00000675667.1:c.492T>C	ENSP00000501803.1:p.Asp164=
ENST00000675874.1:c.357-3651T>C	ENSP00000501851.1:n.357-3651T>C
ENST00000675881.1:c.492T>C	ENSP00000501670.1:p.Asp164=
ENST00000675939.1:c.492T>C	ENSP00000502256.1:p.Asp164=
ENST00000675989.1:n.867T>C
ENST00000676208.1:c.492T>C	ENSP00000502468.1:p.Asp164=
ENST00000676283.1:n.867T>C
ENST00000676385.2:c.492T>C	ENSP00000502091.1:p.Asp164=
ENST00000676434.1:c.492T>C	ENSP00000501648.1:p.Asp164=
ENST00000677389.1:c.492T>C MANE Plus Clinical	ENSP00000503633.1:p.Asp164=
ENST00000347559.6:c.492T>C	ENSP00000292304.3:p.Asp164=
ENST00000361308.8:c.492T>C	ENSP00000355292.5:p.Asp164=
ENST00000368297.5:c.249T>C	ENSP00000357280.1:p.Asp83=
ENST00000368299.7:c.492T>C	ENSP00000357282.3:p.Asp164=
ENST00000368300.8:c.492T>C	ENSP00000357283.4:p.Asp164=
ENST00000368301.6:c.492T>C	ENSP00000357284.2:p.Asp164=
ENST00000448611.6:c.156T>C	ENSP00000395597.2:p.Asp52=
ENST00000469565.6:n.526T>C
ENST00000470199.2:n.434T>C
ENST00000473598.6:c.195T>C	ENSP00000421821.1:p.Asp65=
ENST00000502357.5:n.390T>C
ENST00000502751.5:n.464T>C
ENST00000504687.5:c.243T>C	ENSP00000426535.1:p.Asp81=
ENST00000515459.5:c.*166T>C	ENSP00000424518.1:n.*166T>C
NM_001257374.2:c.156T>C	NP_001244303.1:p.Asp52=
NM_001282624.1:c.249T>C	NP_001269553.1:p.Asp83=
NM_001282625.1:c.492T>C	NP_001269554.1:p.Asp164=
NM_001282626.1:c.492T>C	NP_001269555.1:p.Asp164=
NM_005572.3:c.492T>C , LRG_254t1:c.492T>C	NP_005563.1:p.Asp164=
NM_170707.3:c.492T>C	NP_733821.1:p.Asp164=
NM_170708.3:c.492T>C	NP_733822.1:p.Asp164=
XM_011509533.1:c.156T>C	XP_011507835.1:p.Asp52=
XM_011509534.1:c.-173T>C	XP_011507836.1:n.-173T>C
XR_921781.1:n.741T>C
XM_011509534.2:c.-173T>C	XP_011507836.1:n.-173T>C
XR_921781.2:n.739T>C
NM_170707.4:c.492T>C MANE Select	NP_733821.1:p.Asp164=
NM_001257374.3:c.156T>C	NP_001244303.1:p.Asp52=
NM_001282626.2:c.492T>C	NP_001269555.1:p.Asp164=
NM_001282624.2:c.249T>C	NP_001269553.1:p.Asp83=
NM_001282625.2:c.492T>C	NP_001269554.1:p.Asp164=
NM_005572.4:c.492T>C MANE Plus Clinical	NP_005563.1:p.Asp164=
NM_170708.4:c.492T>C	NP_733822.1:p.Asp164=